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The second part involves 20–30% of the cell death pathway and has characteristics of oxidative glutamate toxicity, because it can be inhibited specifically by vitamin E, group I metabotropic receptor agonists, a caspase inhibitor, elevated extracellular cystine, and the removal of extracellular glutamate (Schubert and Piasecki, 2001)

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For mTYR, the narrow dual copper-binding site makes it more difficult for arbutin, which has two rings, to fit, especially in the MD-stable conformation of Arbutin_b, where the number of hydrogen bonds between arbutin and the pocket is much lower than in other conformations (Table 2)